"Ambry Genetics"[submitter] AND "ADAM9"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1006181	NM_003816.3(ADAM9):c.5G>A (p.Gly2Glu)	ADAM9, LOC130000261 (G2E)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2486380	NM_003816.3(ADAM9):c.61G>C (p.Gly21Arg)	ADAM9, LOC130000261 (G21R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2270731	NM_003816.3(ADAM9):c.71G>A (p.Gly24Asp)	ADAM9, LOC130000261 (G24D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2620755	NM_003816.3(ADAM9):c.196G>A (p.Val66Ile)	ADAM9 (V66I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2237184	NM_003816.3(ADAM9):c.228G>C (p.Glu76Asp)	ADAM9 (E76D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2263945	NM_003816.3(ADAM9):c.466T>C (p.Ser156Pro)	ADAM9 (S156P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2487698	NM_003816.3(ADAM9):c.583C>G (p.Pro195Ala)	ADAM9 (P195A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1352200	NM_003816.3(ADAM9):c.1235A>G (p.Tyr412Cys)	ADAM9 (Y412C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 840132	NM_003816.3(ADAM9):c.1393C>T (p.Arg465Trp)	ADAM9 (R465W)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1958069	NM_003816.3(ADAM9):c.1574A>G (p.Gln525Arg)	ADAM9 (Q525R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1510694	NM_003816.3(ADAM9):c.1600G>C (p.Ala534Pro)	ADAM9 (A534P)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2160555	NM_003816.3(ADAM9):c.1790G>T (p.Gly597Val)	ADAM9 (G597V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 938287	NM_003816.3(ADAM9):c.1871G>C (p.Gly624Ala)	ADAM9 (G624A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 862548	NM_003816.3(ADAM9):c.2065A>G (p.Asn689Asp)	ADAM9 (N689D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1005098	NM_003816.3(ADAM9):c.2429C>T (p.Pro810Leu)	ADAM9 (P810L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1473068	NM_003816.3(ADAM9):c.2444A>G (p.Tyr815Cys)	ADAM9 (Y815C)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GUncertain significance